Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
  • B29B7/00—Mixing; Kneading
  • B29B7/002—Methods
  • B29B7/007—Methods for continuous mixing
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
  • C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
  • C08G63/06—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from hydroxycarboxylic acids
  • C08G63/08—Lactones or lactides
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
  • B29B13/00—Conditioning or physical treatment of the material to be shaped
  • B29B13/04—Conditioning or physical treatment of the material to be shaped by cooling
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
  • B29B13/00—Conditioning or physical treatment of the material to be shaped
  • B29B13/10—Conditioning or physical treatment of the material to be shaped by grinding, e.g. by triturating; by sieving; by filtering
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
  • B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
  • B29C48/001—Combinations of extrusion moulding with other shaping operations
  • B29C48/0018—Combinations of extrusion moulding with other shaping operations combined with shaping by orienting, stretching or shrinking, e.g. film blowing
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
  • B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
  • B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
  • B29C48/07—Flat, e.g. panels
  • B29C48/08—Flat, e.g. panels flexible, e.g. films
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J11/00—Recovery or working-up of waste materials
  • C08J11/04—Recovery or working-up of waste materials of polymers
  • C08J11/10—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation
  • C08J11/12—Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by dry-heat treatment only
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
  • C08J5/18—Manufacture of films or sheets
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
  • B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
  • B29C48/25—Component parts, details or accessories; Auxiliary operations
  • B29C48/285—Feeding the extrusion material to the extruder
  • B29C48/288—Feeding the extrusion material to the extruder in solid form, e.g. powder or granules
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
  • B29K2067/00—Use of polyesters or derivatives thereof, as moulding material
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
  • B29K2067/00—Use of polyesters or derivatives thereof, as moulding material
  • B29K2067/04—Polyesters derived from hydroxycarboxylic acids
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
  • B29K2096/00—Use of specified macromolecular materials not provided for in a single one of main groups B29K2001/00 - B29K2095/00, as moulding material
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
  • B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
  • B29K2105/25—Solid
  • B29K2105/251—Particles, powder or granules
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
  • B29K2995/00—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
  • B29K2995/0037—Other properties
  • B29K2995/004—Semi-crystalline
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
  • B29K2995/00—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
  • B29K2995/0037—Other properties
  • B29K2995/0059—Degradable
  • B29K2995/006—Bio-degradable, e.g. bioabsorbable, bioresorbable or bioerodible
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
  • B29K2995/00—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
  • B29K2995/0037—Other properties
  • B29K2995/0077—Yield strength; Tensile strength
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
  • B29K2995/00—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
  • B29K2995/0037—Other properties
  • B29K2995/0088—Molecular weight
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2367/00—Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
  • C08J2367/04—Polyesters derived from hydroxy carboxylic acids, e.g. lactones
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2467/00—Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
  • C08J2467/04—Polyesters derived from hydroxy carboxylic acids, e.g. lactones

Definitions

• the present disclosure relates generally to polymeric films, and more specifically to polypropiolactone (PPL) films that may be derived from a bio-source.
• PPL films may be suitable for use in various applications, including, for example, packaging applications.
• Conventional polyolefin films are commonly used in many applications. There are many disadvantages in the use of conventional polyolefin films. For instance, conventional polyolefin films are generally not reusable and/or recyclable. Furthermore, the production of conventional polyolefin films requires high temperatures, resulting in a high specific energy consumption process which can be undesirable on scale.
• polypropiolactone (PPL) films are provided herein.
• the resulting films have numerous benefits over conventional polyolefin films.
• the films produced according to the methods herein may undergo extrusion (including, for example, blown film extrusion) at temperatures below that of conventional films with little thermal degradation.
• the films resulting from the methods herein may also be reusable and/or recyclable.
• a method of producing a film comprising cryogenically grinding PPL to form a powder; and extruding the powder to form the film.
• the cryogenically grinding of PPL may involve cryogenically cooling PPL followed by grinding of the cooled PPL.
• the extruding is performed at a temperature between about 80 °C to about 160 °C.
• the powder may undergo melt extrusion, cast extrusion, or blow film extrusion, or any combination thereof, to produce the film.
• a method of producing a film comprising blending a mixture of PPL polymers; and blowing the mixture to form the film.
• the mixture of PPL polymers comprises two or more PPL polymers having different average molecular weight (M w ).
• the resulting film may have a biocontent of at least 60% (w/w) and/or the resulting film may be compostable up to 100%.
• the films described herein may be used as, or further processed into, packaging materials.
• packaging materials may include, for example, shrink wrap.
• a method of producing acrylic acid comprising providing a film according to any of the methods described herein; and thermolyzing at least a portion of the film to produce acrylic acid.
• the film may be produced by cryogenically grinding polypropiolactone (PPL) to form a powder, and extruding the powder to form the film.
• PPL polypropiolactone
• the PPL used to produce the film may be obtained from a bio-source, thereby leading the film produced to be bio-sourced as well.
• the resulting film may also be compostable.
• a method of producing a film comprising cryogenically grinding polypropiolactone (PPL) to form a powder, and extruding the powder to form the film.
• PPL polypropiolactone
• the PPL is a medium molecular weight PPL (MMW PPL). In other embodiments, the PPL is a high molecular weight PPL (HMW PPL).
• the PPL has an average molecular weight (M w ) between about 100,000 g/mol and about 200,000 g/mol. In some variations, the PPL has an average molecular weight (M w ) between about 120,000 g/mol and about 150,000 g/mol. In other variations, the PPL has an average molecular weight (M w ) between about 800,000 g/mol to about 1,000,000 g/mol.
• the PPL used may be obtained from commercially available sources, or produced according to any methods known in the art.
• the PPL may be obtained by polymerizing the BPL to form the PPL.
• the PPL may be obtained by: reacting ethylene oxide with carbon monoxide in the presence of a carbonylation catalyst to form BPL, and polymerizing the BPL to form the PPL.
• the PPL may be obtained by carbonylating ethylene oxide to form BPL, and polymerizing the BPL to form the PPL.
• the PPL used may also be obtained from renewable feedstock.
• renewable feedstock For example, when the PPL is produced from ethylene oxide and carbon monoxide, either or both the ethylene oxide and carbon monoxide may be obtained from renewable feedstock using methods known in the art.
• the PPL is obtained in part or completely from renewable feedstock, the PPL produced from such BPL has a biocontent greater than 0% (w/w).
• biocontent of a material may be measured using the ASTM D6866 method, which allows the determination of the biocontent of materials using radiocarbon analysis by accelerator mass spectrometry, liquid scintillation counting, and isotope mass spectrometry.
• a biocontent result may be derived by assigning 100% equal to 107.5 pMC (percent modem carbon) and 0% equal to 0 pMC. For example, a sample measuring 99 pMC will give an equivalent biocontent result of 93%.
• biocontent may be determined in accordance with ASTM D6866 revision 12 (i.e. , ASTM D6866-12).
• biocontent may be determined in accordance with the procedures of Method B of ASTM- D6866-12.
• Other techniques for assessing the biocontent of materials are described in U.S. Patent Nos. 3,885, 155, 4,427,884, 4,973,841, 5,438,194, and 5,661,299, as well as
• the PPL may be cryogenically ground to form a PPL powder.
• the cryogenic grinding of PPL can occur as a single step or as two steps.
• the cryogenic grinding of PPL involves cryogenic cooling and grinding the PPL in a single step.
• the PPL is cryogenically ground at a temperature between about -50 °C to about -300 °C; between about -50 °C and about -275 °C; between about -50 °C and about -l50°C; between about -100 °C and about -200 °C; or between about -125 °C and about -150 °C.
• combining the cryogenic cooling of the PPL and the grinding of the PPL into a single step may lead to improved blending properties of the PPL powder.
• combining the cryogenic cooling of the PPL and the grinding of the PPL into a single step may yield a film that is produced with little thermal degradation.
• cryogenic grinding of the PPL occurs in two steps.
• the PPL is first cryogenically cooled, and then the cryogenically cooled PPL is ground to form the powder.
• the PPL is cryogenically cooled to a temperature between about -50 °C and about -275 °C; between about -50 °C and about -l50°C; between about -100 °C and about -200 °C; or between about -125 °C and about -150 °C.
• the powder comprises particles of ground PPL. In some embodiments, the powder comprises particles of finely ground PPL. In some embodiments, the powder comprises particles of finely ground PPL of substantially uniform size. In some embodiments, the powder comprises particles having a particle size between about 300 pm and about 3,000 pm; between about 500 pm to about 2,000 pm; or between about 700 pm to about 1,000 pm.
• using a powder comprising particles of finely ground PPL may result in better mixing of the powder.
• using a powder comprising particles of finely ground PPL may help in better feeding of the powder into an extruder.
• the powder produced from the cryogenic grinding of PPL has a specific bulk density.
• the powder has a bulk density suitable for feeding into an extruder.
• the powder produced by cryogenically grinding PPL is extruded to produce a film.
• Various extrusion techniques may be employed to produce the film.
• melt extrusion, cast extrusion, or blow film extrusion may be employed.
• the temperature at which the extrusion is performed may vary depending on the extrusion technique used. For example, in some variations where melt extrusion is employed, the extruding is performed at a temperature range between about 80 °C to about 160 °C.
• a method comprising cryogenically grinding polypropiolactone (PPL) to form a powder; feeding the powder into an extruder; and processing the powder in the extruder to form the film.
• the processing the powder in the extruder comprises melting the powder to form a PPL melt.
• the extruder has a feed temperature of about 10 °C. In other embodiments, the extruder has a barrel temperature between about 50 °C and about 170 °C; or between about 50 °C and about 110 °C. In yet other embodiments, the extruder has a die temperature of between about 110 °C and about 170 °C; or a die temperature of about 110 °C or about 170 °C. In yet other embodiments, the extruder has a film die temperature of between about 110 °C and about 166 °C; or a film die temperature of about 110 °C, about 160 °C, or about 160 °C.
• extruders may be employed in the methods described herein.
• a melt extruder, a parallel twin screw extruder, or an extruder comprising a slit die may be used.
• the PPL melt undergoes minimal thermal decomposition under the extrusion conditions described herein. In one variation, the PPL melt undergoes minimal thermolysis, which would yield acrylic acid, under the extrusion conditions described herein. In one variation, the PPL melt has less than 5%, less than 4%, less than 3%, less than 2%, or less than 1% by weight of acrylic acid. In another variation, less than 5%, less than 4%, less than 3%, less than 2%, or less than 1% by weight of acrylic acid is detected in the PPL melt.
• the powder may be blow molded to produce large diameter and/or width films that may be suitable for use in bulk packaging applications.
• a method of producing a film comprising cryogenically grinding PPL to form a powder, and blow molding the powder to form the film.
• a method of producing a film comprising blending a mixture of PPL polymers; and blowing the mixture to form the film.
• the mixture of PPL polymers comprise two or more, three or more, four or more, or five or more PPL polymers having different average molecular weight (M w ).
• the mixture of PPL polymers comprises two, three or four PPL polymers having different average molecular weight (M w ).
• At least one of the PPL polymers is a medium molecular weight PPL (MMW PPL). In other embodiments, at least one of the PPL polymers is a high molecular weight PPL (HMW PPL). In some variations, at least one of the PPL polymers has an average molecular weight (M w ) between about 100,000 g/mol and about 200,000 g/mol.
• M w average molecular weight
• At least one of the PPL polymers has an average molecular weight (M w ) between about 120,000 g/mol and about 150,000 g/mol. In other variations, at least one of the PPL polymers has an average molecular weight (M w ) between about 800,000 g/mol to about 1,000,000 g/mol.
• a fdm produced according to the foregoing methods is multilayered.
• a fdm produced according to any of the methods described herein.
• a PPL fdm that has a certain biocontent and compostability, as well as certain mechanical and physical properties.
• the fdm produced according to the methods described herein may be obtained from renewable feedstock.
• the PPL used is obtained in part or completely from renewable feedstock, the PPL fdm produced from such PPL has a biocontent greater than 0% (w/w).
• various techniques are known in the art to determine biocontent of a material.
• the fdm has a biocontent of at least 10% (w/w), at least 20% (w/w), at least 30% (w/w), at least 40% (w/w), at least 50% (w/w), at least 60% (w/w), at least 70% (w/w), at least 80% (w/w), at least 90% (w/w), at least 95% (w/w), at least 96% (w/w), at least 97% (w/w), at least 98% (w/w), at least 99% (w/w), at least 99.5% (w/w), at least 99.9% (w/w), at least 99.99% (w/w), or 100% (w/w); or between about 80% (w/w) and about 100% (w/w), between about 90% (w/w) and about 100% (w/w), or between about 95% (w/w) and about 100% (w/w).
• the fdm produced according to the methods herein has compostability characteristics that are superior to conventional fdms, including conventional polyolefin fdms.
• the fdm may be compostable up to 10%, up to 20%, up to 30%, up to 40%, up to 50%, up to 60%, up to 70%, up to 80%, up to 90%, or up to 100%; or between about 80% and about 100%, between about 90% and about 100%, or between about 95% and about 100%.
• the film has a tensile modulus between about 800 MPa and 1100 MPa; or between about 835 MPa and about 1065 MPa. In other embodiments, the film has a tensile modulus between about 0.5 GPa and about 3.6 GPa; between about 1 GPa and 1.5 GPa, or between about 1 GPa and 1.1 GPa.
• the film has a tensile strength at break between about 20 MPa and about 35 MPa; or between about 25 MPa and about 35 MPa. In other embodiments, the film has a tensile strength at break between about 5 MPa and about 50 MPa; between about 10 MPa and 40 MPa; or between about 20 MPa and about 30 MPa.
• the film has an elongation at break between about 300% and 800%; between about 400% and about 700%; or between about 440% and about 660%.
• the film has an elongation at break between about 0.1% and 1000%; between about 50% and 700%; between 100% and 700%; between 200% and 600%; between about 500% and 700%; or between about 600% and about 700%.
• the film has a glass transition temperature (T g ) between about -l50°C and about 70 °C; between about -50°C and about 0 °C; or between about -30 °C and about -10 °C; or about -20°C.
• T g glass transition temperature
• the film has a melt temperature (T m ) between about 50 °C and about l80°C; between about 60 °C and about 150 °C; between about 70 °C and l00°C; or between about 70°C and about 80°C.
• T m melt temperature
• the film has up to about 50 % crystallinity.
• crystallinity is measured by Differential Scanning Calorimetry.
• the film is uniform.
• the film is multilayered.
• a film having: (a) a biocontent of at least 90%; (b) a tensile modulus between about 835 MPa and about 1065 MPa, (c) a tensile strength at break range between about 25 MPa and about 35 MPa, or (d) an elongation at break range of about 440 % to about 660 %, or any combination of (a)-(d).
• reference to“about” a value or parameter herein includes (and describes) embodiments that are directed to that value or parameter per se.
• description referring to“about x” includes description of“x” per se.
• the term“about” when used in association with other measurements, or used to modify a value, a unit, a constant, or a range of values refers to variations of +/- 10%.
• reference to“between” two values or parameters herein includes (and describes) embodiments that include those two values or parameters per se.
• description referring to“between x and y” includes description of“x” and “y” per se.
• the PPL film described herein may be recyclable and/or reusable, and may be suitable for use in various applications.
• the PPL film may be used in packaging (e.g., in packaging manufactured goods).
• packaging e.g., in packaging manufactured goods.
• the film is used as, or further processed into, packaging material.
• the film is used as shrink wrap.
• Such film may be a recyclable shrink wrap.
• the film may undergo thermolysis to produce acrylic acid.
• packaging material may be used to produce acrylic acid.
• a method of producing acrylic acid comprising:
• One film was produced from medium molecular weight PPL, and another film was produced from high molecular weight PPL according to the following general procedure.
• PPL was cryogenically ground to obtain a powder of desired bulk density, suitable for feeding into an extruder. Both lots of PPL powder were melt extruded into films using a parallel twin screw extruder in separate extrusion trials. Processing temperatures for PPL vary from 80°C to l60°C, which is generally much lower than other thermoplastic resins used in film applications. Such processing temperatures can lead to significant savings in energy in commercial production. During extrusion, there was no acrylic acid odor detected, thus suggesting there was no apparent thermal degradation of the PPL during the extrusion process.
• MMW PPL refers to the PPL film prepared from the medium molecular weight PPL HMW PPL refers to the PPL film prepared from the high molecular weight PPL
• a PPL film was produced in general accordance with the procedure set forth in Example 1 above. PPL was melt extruded to produce a film having the following properties summarized in Table 2 below.

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• 2019
  • 2019-04-01 EP EP19782143.2A patent/EP3774987A4/de active Pending
  • 2019-04-01 JP JP2020543848A patent/JP2021517521A/ja active Pending
  • 2019-04-01 WO PCT/US2019/025184 patent/WO2019195168A1/en active Application Filing
  • 2019-04-01 US US16/970,736 patent/US11773215B2/en active Active
  • 2019-04-01 CN CN201980019737.9A patent/CN111868138A/zh active Pending
  • 2019-04-03 TW TW108111854A patent/TW201943537A/zh unknown
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